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FDA 510(k)

VITAFLOW SUCTION/ASPIRATION TUBING SET

K-Number: K960616 · 1996-05-06

Decision Date1996-05-06
Product CodeBYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VITAFLOW SUCTION/ASPIRATION TUBING SET is the device name listed in this FDA 510(k) record. The listed applicant is Vital Concepts, Inc.. It received FDA 510(k) clearance on 1996-05-06 under 510(k) number K960616. The device is classified under product code BYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITAFLOW SUCTION/ASPIRATION TUBING SET?

VITAFLOW SUCTION/ASPIRATION TUBING SET is a medical device that received FDA 510(k) clearance on 1996-05-06. The listed applicant is Vital Concepts, Inc.. The 510(k) number is K960616.

When did VITAFLOW SUCTION/ASPIRATION TUBING SET receive FDA 510(k) clearance?

VITAFLOW SUCTION/ASPIRATION TUBING SET received FDA 510(k) clearance on 1996-05-06, under 510(k) number K960616.

Who is the listed applicant for VITAFLOW SUCTION/ASPIRATION TUBING SET?

The FDA 510(k) record lists Vital Concepts, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITAFLOW SUCTION/ASPIRATION TUBING SET?

The FDA product code for VITAFLOW SUCTION/ASPIRATION TUBING SET is BYY.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Vital Concepts, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: BYY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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